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(E)-3-(4-tert-butylphenyl)-N-[3-fluoro-4-(methylsulfonamido)benzyl]-3-phenylacrylamide

Base Information Edit
  • Chemical Name:(E)-3-(4-tert-butylphenyl)-N-[3-fluoro-4-(methylsulfonamido)benzyl]-3-phenylacrylamide
  • CAS No.:1450760-15-2
  • Molecular Formula:C27H29FN2O3S
  • Molecular Weight:480.603
  • Hs Code.:
  • Mol file:1450760-15-2.mol
(E)-3-(4-tert-butylphenyl)-N-[3-fluoro-4-(methylsulfonamido)benzyl]-3-phenylacrylamide

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (E)-3-(4-tert-butylphenyl)-N-[3-fluoro-4-(methylsulfonamido)benzyl]-3-phenylacrylamide Edit
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Technology Process of (E)-3-(4-tert-butylphenyl)-N-[3-fluoro-4-(methylsulfonamido)benzyl]-3-phenylacrylamide

There total 6 articles about (E)-3-(4-tert-butylphenyl)-N-[3-fluoro-4-(methylsulfonamido)benzyl]-3-phenylacrylamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 5 steps
1.1: tetrahydrofuran; diethyl ether / 2 h / -78 °C
2.1: dipyridinium dichromate / dichloromethane / 12 h / 20 °C / Molecular sieve
3.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C / Inert atmosphere
3.2: 12 h / 0 - 20 °C / Inert atmosphere
4.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 1 h / 20 °C
5.1: triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; 4-methyl-morpholine / tetrahydrofuran / 14 h
With 4-methyl-morpholine; dipyridinium dichromate; lithium hydroxide monohydrate; sodium hydride; triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In tetrahydrofuran; diethyl ether; dichloromethane; water; mineral oil;
DOI:10.1007/s12272-013-0228-x
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C / Inert atmosphere
1.2: 12 h / 0 - 20 °C / Inert atmosphere
2.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 1 h / 20 °C
3.1: triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; 4-methyl-morpholine / tetrahydrofuran / 14 h
With 4-methyl-morpholine; lithium hydroxide monohydrate; sodium hydride; triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In tetrahydrofuran; water; mineral oil;
DOI:10.1007/s12272-013-0228-x
Guidance literature:
Multi-step reaction with 4 steps
1.1: dipyridinium dichromate / dichloromethane / 12 h / 20 °C / Molecular sieve
2.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 0 °C / Inert atmosphere
2.2: 12 h / 0 - 20 °C / Inert atmosphere
3.1: lithium hydroxide monohydrate / tetrahydrofuran; water / 1 h / 20 °C
4.1: triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; 4-methyl-morpholine / tetrahydrofuran / 14 h
With 4-methyl-morpholine; dipyridinium dichromate; lithium hydroxide monohydrate; sodium hydride; triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In tetrahydrofuran; dichloromethane; water; mineral oil;
DOI:10.1007/s12272-013-0228-x
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